Dein persönlicher KI-Karriere-Agent
Site Quality Head(m/w/x)
Directing QA staff and strategic quality initiatives for GMP pharmaceutical production. 10 years in GMP pharmaceutical manufacturing experience required. Global project team collaboration.
Anforderungen
- BS/MSc in Life Sciences or related experience
- 10 years of experience in GMP Pharmaceutical Manufacturing
- At least 3 years in Quality Control and/or Quality Assurance
- Proven track record in supporting Quality Control operations
- In-depth knowledge of cGMP and FDA regulations
- Ability to manage multiple projects with moderate complexity
- Highly developed management and communication skills
- Strong organizational and time management skills
- Experience in process improvement approaches
Aufgaben
- Provide leadership for strategic site initiatives
- Represent site quality in local and global project teams
- Support and direct the Quality Assurance department staff
- Ensure staff are qualified, competent, and motivated
- Create user requirements and specifications for projects
- Coordinate with stakeholders for clear communication
- Ensure facilities and equipment are safe and compliant
- Oversee project planning, construction, and qualification
- Maintain updated project plans to track progress
- Escalate risks related to timelines and budgets
- Manage product critical quality issues and deviations
- Ensure effective execution of investigations and CAPAs
- Define and monitor Site Quality KPIs
- Establish and oversee the Site Quality Committee
- Coordinate the execution of Site Quality Plans and assessments
- Prepare and consolidate the Quality Unit budget
- Ensure adherence to health and safety procedures
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Lean Six Sigma
- Total Quality Management
- 5S
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Site Quality Head(m/w/x)
Directing QA staff and strategic quality initiatives for GMP pharmaceutical production. 10 years in GMP pharmaceutical manufacturing experience required. Global project team collaboration.
Anforderungen
- BS/MSc in Life Sciences or related experience
- 10 years of experience in GMP Pharmaceutical Manufacturing
- At least 3 years in Quality Control and/or Quality Assurance
- Proven track record in supporting Quality Control operations
- In-depth knowledge of cGMP and FDA regulations
- Ability to manage multiple projects with moderate complexity
- Highly developed management and communication skills
- Strong organizational and time management skills
- Experience in process improvement approaches
Aufgaben
- Provide leadership for strategic site initiatives
- Represent site quality in local and global project teams
- Support and direct the Quality Assurance department staff
- Ensure staff are qualified, competent, and motivated
- Create user requirements and specifications for projects
- Coordinate with stakeholders for clear communication
- Ensure facilities and equipment are safe and compliant
- Oversee project planning, construction, and qualification
- Maintain updated project plans to track progress
- Escalate risks related to timelines and budgets
- Manage product critical quality issues and deviations
- Ensure effective execution of investigations and CAPAs
- Define and monitor Site Quality KPIs
- Establish and oversee the Site Quality Committee
- Coordinate the execution of Site Quality Plans and assessments
- Prepare and consolidate the Quality Unit budget
- Ensure adherence to health and safety procedures
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Lean Six Sigma
- Total Quality Management
- 5S
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Novartis Business Services GmbH
Branche
Pharmaceuticals
Beschreibung
The company is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities it serves.
Noch nicht perfekt?
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